Detail of > 106930-51-2
- CAS Number:
- 106930-51-2
- Name:
Carbamic acid,N-[(1R)-1-(hydroxymethyl)-3-methylbutyl]-, 1,1-dimethylethyl ester
- Superlist Name:
- Boc-D-Leucinol
- Formula:
- C11H23NO3
- Molecular Structure:
![Molecular Structure of 106930-51-2 (Carbamic acid,N-[(1R)-1-(hydroxymethyl)-3-methylbutyl]-, 1,1-dimethylethyl ester)](http://www.lookchem.com/300w/2010/0612/106930-51-2.jpg)
- Synonyms:
- Carbamicacid, [(1R)-1-(hydroxymethyl)-3-methylbutyl]-, 1,1-dimethylethyl ester (9CI);Carbamic acid, [1-(hydroxymethyl)-3-methylbutyl]-, 1,1-dimethylethyl ester,(R)-;Boc-D-Leu-OL;Boc-D-Leucinol;
- Molecular Weight:
- 217.31
- Density:
- 0.984 g/cm3
- Boiling Point:
- 319.3 °C at 760 mmHg
- Flash Point:
- 146.9 °C
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Reference
- New methods and reagents in organic synthesis
- New methods and reagents in organic synthesis. 61. Synthetic studies on ascidiacyclamide and ulithiacyclamide, cytotoxic cyclic peptides from marine tunicates. Kato, Shinji; Kondo, Yutaka; Sugiura, Tsuneyuki; Hamada, Yasumasa; Shioiri, Takayuki (Fac. Pharm. Sci.There are some reagents with their cas registry numbers 106930-51-2 and 100803-72-3 are used in this study., Nagoya City Univ., Nagoya 467, Japan). Pept. Chem., Volume Date 1985, 23rd, 67-72 (English) 1986. CODEN: PECHDP. ISSN: 0388-3698. DOCUMENT TYPE: Journal CA Section: 34 (Amino Acids, Peptides, and Proteins) Two alternative syntheses of ascidiacyclamide (I) and the first synthesis of ulithiacyclamide (II) are described. The multistep procedures start with thiazole amino acids III (Boc = Me3CO2C; R = Me2CH, Me2CHCH2), which are available from Boc-Val-OH and Boc-Leu-OH. .
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